Multiple Sclerosis Flashcards

1
Q

What is the pathophysiology of multiple sclerosis?

A

Cell mediated autoimmune demyelination of the white matter CNS. This leads to reduced conduction velocity
Disseminated (over time and space)

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2
Q

What are some poor prognostic signs for MS?

A

Older patient
Motor signs at onset
Many MRI lesions

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3
Q

What are common first symptoms of MS?

A

Optic Neuritis - pain on eye movement with greying and blurring of vision
Odd sensations such as wetness or burning

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4
Q

What pathway does MS commonly involve?

A

Corticospinal path - motor pathway

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5
Q

How does heat affect MS symptoms?

A

Symptoms worsen

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6
Q

What sensory symptoms are seen in MS?

A
Dysaesthesia (abnormal unpleasant feeling when touched)
Pins and needles
Decreased vibration sense
Trigeminal neuralgia
Lhermitte's syndrome
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7
Q

What motor symptoms are seen in MS?

A

Spastic weakness
Myelitis
Hyper-reflexia

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8
Q

What GU symptoms are seen in MS?

A

Erectile dysfunction
Anorgasmia
Urinary frequency
Incontinence

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9
Q

What GI symptoms are seen in MS?

A

Swallowing difficulty

Constipation/diarrhoea

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10
Q

What eye symptoms are seen in MS?

A
Diplopia
Optic neuritis
Nystagmus
Opthalmoplegia
Uhthoff's Phenomenon
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11
Q

What cerebellar signs are seen in MS?

A

Trunk/limb ataxia
Intention tremor
Scanning speech (ataxic dysarthria)

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12
Q

What cognitive/visiospatial signs are seen in MS?

A

Amnesia
Executive dysfunction - emotional and behavioural difficulty
Depression/mood disorders
cognitive impairment

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13
Q

What are some subtypes of MS?

A

Relapsing-remitting (most common)
Secondary progressive disease
Primary progressive disease

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14
Q

What is relapsing-remitting MS like?

A

Acute 1-2 month attacks followed by periods of remission

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15
Q

What is secondary progressive disease?

A

R-R patients don’t fully remit and over time the disability accumulates (around 65% of R-R patients progress within 15 years)

See gait and bladder problems

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16
Q

What is primary progressive disease?

A

Progressive deterioration seen from the onset

17
Q

What is Lhermitte’s syndrome?

A

electric shocks in limbs on neck flexion

18
Q

What is Uhthoff’s phenomenon?

A

Worsening vision following rise in temperature

19
Q

What lifestyle advice is given for patients with MS?

A

Regular exercise
Stop smoking
Avoid stressful situations

20
Q

How are acute relapses managed?

A

High dose IV methylprednisolone

21
Q

What criteria have to be met for beta interferon to be used?

A

Not suitable for primary progressive.

Have to have had 2 relapses in past 2 years.

22
Q

What is the effect of beta interferon on MS?

A

Reduce number of relapses and MRI changes

No effect on disability

23
Q

What disease modifying drugs are used in MS

A
Interferon-B
Glatiramer acetate
Dimethyl fumerate
Alemtuzumab
Natalizumab
Fingolimod
24
Q

How is spasticity in MS controlled?

A

Baclofen and gabapentin

Physio

25
How is tremor in MS controlled?
Botulinum toxin | Primidone
26
How is bladder dysfunction managed?
If significant residual volume - self catheterise | Frequency symptoms - Anticholinergics
27
How is oscillopsia (visual fields oscillating) managed?
Gabapentin
28
How is fatigue managed?
Amantadine and CBT
29
How is MS diagnosed? What are the results of these investigations?
MRI contrast: demyelination plaques (hyperintense plaques in the periventricular region) Electrophoresis of CSF: oligoclonal bands of IgG Evoked potentials: prolonged conduction
30
Differentials for MS
Cervical spondylosis Fibromyalgia Stroke B12 deficiency